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Daily review of charts to determine if pre-certification/pre-authorization or referrals are needed. To ensure procurement of accurate pre-certification authorization/referral for applicable returning and new patients as well as review and completion of accurate, complete patient charts.
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Serve as a liaison with the PI and I-SCREEN Grant Administrator for budgeting, contracting and financial oversight with external sponsors and internal offices, developing annual study budgets as needed, reviewing study financials monthly, and addressing any budgetary shortfalls in a timely manner with the I-SCREEN PI.
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The Physician will be assigned to provide weekly review and oversight of blood glucose management of patients with diabetes mellitus (types 1 and 2), as well as initial consults on patients admitting with diagnoses such as diabetes mellitus, thyroid disease, growth hormone deficiency, and other conditions including but not limited to Turner’s Syndrome, cystic fibrosis-related diabetes, and inborn errors of metabolism.
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Reviews chart review worksheets completed by the nursing staff, making corrections/suggestions as needed. Functions as a working Nursing Manager, taking on the role of admitting nurse, procedural nurse or recovery room nurse as needed.
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Review all vendor shop installations with New Store/ Renovation Manager as needed. Create Art Production Request Forms and provide images as needed. Participate in Prototype process as needed.
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Review occupational dosimetry reports for radiation workers, and consult as needed when ALARA levels are exceeded, or when there is concern about occupational exposure. Advise, support, and consult with technologists, radiologists, and Radiation Safety Officer (RSO) regarding clinical protocol management, dose assessment, and review of Radiation Protection Program Elements.
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Organizes and directs plan review meetings as needed with architects, engineers, contractors, builders, property owners, and the public. Provides timely response to requests for information from clients; provides assistance and information to residents, developers, contractors, attorneys, and County officials regarding planning/zoning issues, land use issues, code/ordinance interpretations, development policies, site plans, plan reviews, review procedures, permits, fees, documentation, zoning conditions compliance or other issues; responds to questions/complaints, researches problems, and initiates problem resolution.
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Work with Cad Designers to develop original textile and embroidery designs•Design according to style plans, sales needs and emerging trends; ensure timely execution of product development calendar•Create Illustrator sketches; review line sheets; develop tech packs•Build 3-D bodies•Source, select and review raw materials and trims ensure they are within price points•Review styles with costing engineer to design into price points needed.
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The scientist will work flexibly across a variety of projects and have expertise or proficiency in Pharmacokinetics (PK)/pharmacodynamics (PD) including PK study design, data analysis, data review and bioanalysis in support of the Company’s pipeline, IND/CTA and NDA submissions.
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Assist internal acquisition teams with potential mergers and acquisitions by performing due diligence, synthesizing and presenting data as needed for applicable M&A targets, and drafting schedules, post-closing integration documents, other transactional documents as needed.
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The Lead Clinical Laboratory Scientist is a Licensed Medical Technologist whose primary responsibilities are to train others, perform laboratory testing on patients samples, review QC and perform troubleshooting as needed.
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This individual specializes in deviation prevention by executing QA on-the-floor activities that include but are not limited to in-process batch record review, logbook review, GEMBAs of all manufacturing areas, providing feedback to colleagues, observing active processes, supporting Manufacturing and PE by providing Quality input as needed, and requesting the initiation of deviations as they are identified.
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Prepare and provide input to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, regulatory responses)Participate or lead as needed the review and assessment of new opportunities and ESRs. Responsible for timely responses to investigational study sites for local ICF changes, protocol & EC/IRB questions/requests.
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If reasonable accommodation is needed to participate in the job application or interview process or to perform essential job duties, please contact our HR Dept. KEYS: Party Chief, Land Surveyor, Roadway/Heavy Civil Education Bachelor's Degree Preferred Certification Required.
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Generate a Loan Review work paper as a result of the duties outlined above as well as other reports as needed to fully analyze each credit assigned in the portfolio. Experience using Jack Henry/Silverlake, Global Wave Portfolio Track and DiCOM Loan Review software preferred, but not required.
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